Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:43389763-43389955 | Not yet | Common:3; Rare:85 | 310 | ||
chr1:43946629-43946987 | Not yet | Rare:96 | 273 | ||
chr1:44674401-44674756 | Not yet | Common:3; Rare:97 | 379 | ||
chr1:44739641-44739941 | Not yet | Common:3; Rare:124 | 347 | ||
chr1:44775445-44775607 | Not yet | Rare:61 | 199 | ||
chr1:44986532-44986733 | Not yet | Common:2; Rare:38; Clinvar (benign):1 | 206 | ||
chr1:45339996-45340212 | Not yet | Rare:76; Clinvar:1; Clinvar (benign):3 | 248 | ||
chr1:45500056-45500358 | Not yet | Common:1; Rare:74; Clinvar:4; Clinvar (pathogenic):3 | 334 | ||
chr1:45521833-45522087 | Not yet | Common:1; Rare:100 | 260 | ||
chr1:45550730-45551112 | Not yet | Common:3; Rare:93 | 382 | ||
chr1:45583931-45584078 | Not yet | Rare:57 | 261 | ||
chr1:45687059-45687351 | Not yet | Common:1; Rare:75 | 315 | ||
chr1:45688059-45688211 | Not yet | Common:1; Rare:39 | 283 | ||
chr1:45750618-45750793 | Not yet | Rare:66 | 139 | ||
chr1:46132622-46132774 | Not yet | Rare:54 | 204 |